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Acetic Acid → HCID 53728512, 화합물

HRID 2413740
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HRID 2413740 반응식
[CH3:1][N:2]([CH3:7])[C:3](=[S:6])[NH:4][NH2:5].[C:8]([C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([C:17](=O)[CH3:18])[N:12]=1)(=O)[CH3:9].C(O)(=O)C>CCO>[CH3:1][N:2]([CH3:7])[C:3](=[S:6])[NH:4][N:5]=[C:8]([C:11]1[N:12]=[C:13]([C:17](=[N:5][NH:4][C:3]([N:2]([CH3:7])[CH3:1])=[S:6])[CH3:18])[CH:14]=[CH:15][CH:16]=1)[CH3:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 707902,6-DiacetylpyridineHCID 27337003-Amino-1,1-dimethylthiourea

생성물 1

HCID 53728512HCID 53728512, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 4,4-dimethylthiosemicarbazide (2.70 g, 0.022 mol) and 2,6-diacetylpyridine (1.63 g, 0.10 mol) in 95% EtOH (45 ml) containing glacial acetic acid (0.5 ml) was heated by a steam bath for 1 h and 10 min and allowed to cool to ambient temperature. The yellow precipitate was collected by filtration, washed with 95% EtOH, and subsequently recrystallized from toluene: yield 2.72 g (73%); mp 215° (dec).

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후처리

  1. temperaturewas heated by a steam bath for 1 h and 10 min
  2. filtrationThe yellow precipitate was collected by filtration
  3. washwashed with 95% EtOH
  4. customsubsequently recrystallized from toluene

출처 및 근거

ORD 기록
ord-a0af7a1eca7442dcac6efbdf88b9d9c5
출처 데이터셋
uspto-grants-1988_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04719221

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